NDC product
GUNA SLEEP SUPPORT
NDC 17089-471 · Guna spa
Key facts
| Product NDC | 17089-471 |
|---|---|
| Proprietary name | GUNA SLEEP SUPPORT |
| Nonproprietary name | avena sativa flowering top - caffeine - matricaria chamomilla whole - Passiflora incarnata flowering top -potassium bromide - zinc valerate dihydrate - silver nitrate - strychnos ingatii seed - |
| Substances | POTASSIUM BROMIDE, CAFFEINE, AVENA SATIVA FLOWERING TOP, MATRICARIA CHAMOMILLA WHOLE, STRYCHNOS IGNATII SEED, PASSIFLORA INCARNATA FLOWERING TOP, SILVER NITRATE, ZINC VALERATE DIHYDRATE |
| Dosage form | SOLUTION/ DROPS |
| Route | ORAL |
| Labeler | Guna spa |
| Product type | HUMAN OTC DRUG |
| Marketing category | UNAPPROVED HOMEOPATHIC |
| Pharmacologic classes | Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE], Methylxanthine [EPC], Xanthines [CS] |
| Marketing start | Jan 17, 2021 |
| Listing certified through | Dec 31, 2027 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date: